A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565752



Internal ID7037134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:152585635..152589649hg38UCSC Ensembl
Outerchr3:152303424..152307438hg19UCSC Ensembl
Outerchr3:153786114..153790128hg18UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg384015
hg194015
hg184015
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv990765
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565752
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer